Canonical Allele Identifier: PA2827474162
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser39Pro
CA16616578
NM_001349956.2:c.115T>C